Rangariroyashe H. Chipika on Muck Rack

Rangariroyashe H. Chipika

As seen in: Wiley Online Library, MDPI
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Articles

Sensory Dysfunction in ALS and Other Motor Neuron Diseases: Clinical Relevance, Histopathology, Neurophysiology, and Insights from Neuroimaging

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By Jana Kleinerova, Rangariroyashe H. Chipika, Yana Yunusova, Véronique Marchand-Pauvert
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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The involvement of language‐associated networks, tracts, and cortical regions in frontotemporal dementia and amyotrophic lateral sclerosis: Structural and functional alterations

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By Marlene Tahedl, Rangariroyashe H. Chipika, Jennifer C. Hengeveld, Jasmin Lope
| Wiley Online Library Verified
1 INTRODUCTION The clinical profile of amyotrophic lateral sclerosis (ALS) is classically associated with bulbar dysfunction, respiratory weakness, decline in dexterity, and gait impairment (Yunusova et al., 2019).
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Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations

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By Peter Bede, Rangariroyashe H. Chipika, Foteini Christidi, Jennifer C. Hengeveld
| bmj.com
Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations http://orcid.org/0000-0003-0492-4772Peter Bede1, Rangariroyashe H. Chipika1, http://orcid.org/0000-0003-1297-9415Foteini Christidi1,2, Jennifer C. Hengeveld3, Efstratios Karavasilis2, Georgios D. Argyropoulos2, Jasmin Lope1, Stacey Li Hi Shing1, Georgios Velonakis2, Léonie Dupuis3,4, Mark A. Doherty3, Alice Vajda3, Russell L.
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